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1

Nationalism in exile: Nationalism among Moluccans in The Netherlands 1951–1990

Steijlen, Fridus

Journal:

History of European Ideas

Year:

1992

Language:

english

File:

PDF, 508 KB

english, 1992

2

基底细胞癌的遗传学分析

Reinders, M.G.H.C., Cosgun, B., Gijezen, L.M.C., Oosterhoud, C.N., Kelleners‐Smeets, N.W.J., Vermander, E., Vreeburg, M., Steijlen, P.M., Mosterd, K., Geel, M.

Journal:

British Journal of Dermatology

Year:

2019

File:

PDF, 151 KB

2019

3

New type of twin spot

M.A.M. van Steensel, P.M. Steijlen, M.B. Maessen-Visch

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 174 KB

english, 2005

4

Lymphedema, cardiac septal defects, and characteristic facies: Possible new case of Irons–Bianchi syndrome

M.A.M. van Steensel, M. van Geel, C. Schrander-Stumpel, P.M. Steijlen, J.C.J.M. Veraart

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 161 KB

english, 2007

5

Extensive capillary malformation with a compensated coagulopathy

Bousema, H. Kramer, Steijlen

Journal:

Clinical and Experimental Dermatology

Year:

1999

Language:

english

File:

PDF, 196 KB

english, 1999

6

Naevus corniculatus: a new acantholytic disorder

R. HAPPLE, P.M. STEIJLEN, G. KOLDE

Journal:

British Journal of Dermatology

Year:

1990

Language:

english

File:

PDF, 1.47 MB

english, 1990

7

Effect of topical calcipotriol on congenital ichthyoses

G.P.H. LUCKER, P.C.M. Van De KERKHOF, M.R. Van DÏJK, P.M. STEIJLEN

Journal:

British Journal of Dermatology

Year:

1994

Language:

english

File:

PDF, 1.71 MB

english, 1994

8

Phenotypic variability associated with WNT10A nonsense mutations

M. Van Geel, M. Gattas, Y. Kesler, P. Tong, H. Yan, K. Tran, P.M. Steijlen, D.F. Murrell, M.A.M. Van Steensel

Journal:

British Journal of Dermatology

Year:

2010

Language:

english

File:

PDF, 641 KB

english, 2010

9

A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome

E.A. de Zwart-Storm, M. van Geel, E. Veysey, S. Burge, S. Cooper, P.M. Steijlen, P.E. Martin, M.A.M. van Steensel

Journal:

British Journal of Dermatology

Year:

2011

Language:

english

File:

PDF, 317 KB

english, 2011

10

Clinically manifest X-linked recessive ichthyosis in a female due to a homozygous interstitial 1·6-Mb deletion of Xp22.31

I.F. Nagtzaam, A.P.A. Stegmann, P.M. Steijlen, J. Herbergs, J.A. Van Lent-Albrechts, M. Van Geel, M.A.M. Van Steensel

Journal:

British Journal of Dermatology

Year:

2012

Language:

english

File:

PDF, 199 KB

english, 2012

11

Cancer-related secondary lymphoedema due to cutaneous lymphangitis carcinomatosa: clinical presentations and review of literature

R.J. DAMSTRA, E.A. JAGTMAN, P.M. STEIJLEN

Journal:

European Journal of Cancer Care

Year:

2010

Language:

english

File:

PDF, 1.68 MB

english, 2010

12

Aplasia cutis congenita and associated disorders: an update

Mirjam E. J. W. Evers, Peter M. Steijlen, Ben C. J. Hamel

Journal:

Clinical Genetics

Year:

1995

Language:

english

File:

PDF, 510 KB

english, 1995

13

Seed regeneration of Scots pine in boreal forest stands dominated by lichen and feather moss

Steijlen, Ingeborg, Nilsson, Marie-Charlotte, Zackrisson, Olle

Journal:

Canadian Journal of Forest Research

Year:

1995

Language:

english

File:

PDF, 189 KB

english, 1995

14

Photodynamic therapy vs. topical imiquimod for treatment of superficial basal cell carcinoma: a subgroup analysis within a noninferiority randomized controlled trial

Roozeboom, M.H., Nelemans, P.J., Mosterd, K., Steijlen, P.M., Arits, A.H.M.M., Kelleners-Smeets, N.W.J.

Journal:

British Journal of Dermatology

Year:

2015

Language:

english

File:

PDF, 210 KB

english, 2015

15

Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype

Oji, V., Hautier, J. M., Ahvazi, B., Hausser, I., Aufenvenne, K., Walker, T., Seller, N., Steijlen, P. M., Kuster, W., Hovnanian, A., Hennies, H. C., Traupe, H.

Journal:

Human Molecular Genetics

Year:

2006

Language:

english

File:

PDF, 3.63 MB

english, 2006

16

Sjogren-Larsson syndrome: Clinical and MRI/MRS findings in FALDH-deficient patients

van Domburg, P. H. M. F., Willemsen, M. A. A. P., Rotteveel, J. J., de Jong, J. G. N., Thijssen, H. O. M., Heerschap, A., Cruysberg, J. R. M., Wanders, R. J. A., Gabreels, F. J. M., Steijlen, P. M.

Journal:

Year:

1999

Language:

english

File:

PDF, 1.53 MB

english, 1999

17

Diphencyprone in the Management of Refractory Palmoplantar and Periungual Warts: An Open Study

Rampen, F.H.J., Steijlen, P.M.

Journal:

Year:

1996

File:

PDF, 1.21 MB

1996

18

Prevalence of Symptomatic Intracranial Aneurysm and Ischaemic Stroke in Pseudoxanthoma Elasticum

vandenBerg, JanS.P., Hennekam, Raoul C.M., Cruysberg, Jan R.M., Steijlen, Peter M., Swart, Jaap, Tijmes, Nel, Limburg, Martien

Journal:

Cerebrovascular Diseases

Year:

2000

Language:

english

File:

PDF, 172 KB

english, 2000

19

An Inertial Measurement Unit Based Method to Estimate Hip and Knee Joint Kinematics in Team Sport Athletes on the Field

Bastiaansen, Bram J.C., Wilmes, Erik, Brink, Michel S., de Ruiter, Cornelis J., Savelsbergh, Geert J.P., Steijlen, Annemarijn, Jansen, Kaspar M.B., van der Helm, Frans C.T., Goedhart, Edwin A., van de

Journal:

Journal of Visualized Experiments

Year:

2020

File:

PDF, 573 KB

2020

20

Hypomelanosis of Ito: A symptom, not a syndrome

van Steensel, M.A.M., Steijlen, P.M.

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 30 KB

english, 1998

21

Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes

Steijlen, Peter M., van Steensel, Maurice A.M.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 60 KB

english, 1999

22

Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots

Han G. Brunner, Theo Hulsebos, Peter M. Steijlen, Daan J. der Kinderen, A. v.d. Steen, Ben C. J. Hamel

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 305 KB

english, 1993

23

Variant of odontoonychodermal dysplasia?

W. P. Arnold, M. A. W. Merkx, P. M. Steijlen

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 304 KB

english, 1995

24

A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma

M.A.M. van Steensel, L. Spruijt, I. van der Burgt, R.S. Bladergroen, M. Vermeer, P.M. Steijlen, M. van Geel

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 163 KB

english, 2005

25

Myhre syndrome in a female with previously undescribed symptoms: Further delineation of the phenotype

M.A.M. van Steensel, M. Vreeburg, P.M. Steijlen, C. de Die-Smulders

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 204 KB

english, 2005

26

A case of Lelis syndrome with hystrix-like ichthyosis

M.A.M. van Steensel, V. Winnepenninckx, I.F. Nagtzaam, R. Janssens, R. De Vos, P.M. Steijlen

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 338 KB

english, 2008

27

Molecular genetics of hereditary hair and nail disease

M.A.M. van Steensel, M. van Geel, P.M. Steijlen

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2004

Language:

english

File:

PDF, 208 KB

english, 2004

28

Novel missense mutations in the FOXC2 gene alter transcriptional activity

M.A.M. van Steensel, R.J. Damstra, M. Heitink, R.S. Bladergroen, J. Veraart, Peter M. Steijlen, M. van Geel

Journal:

Year:

2009

Language:

english

File:

PDF, 174 KB

english, 2009

29

Acrodermatitis continua of Hallopeau in a patient with myelodysplastic syndrome

P.C.M. van der KERKHOF, P.M. STEIJLEN, R.A.P. RAYMAKERS

Journal:

British Journal of Dermatology

Year:

1996

Language:

english

File:

PDF, 1.84 MB

english, 1996

30

Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1

F.J.D. Smith, M. Del Monaco, P.M. Steijlen, C.S. Munro, M. Morvay, C.M. Coleman, F.J.R. Rietveld, J. Uitto, W.H.I. Mclean

Journal:

British Journal of Dermatology

Year:

1999

Language:

english

File:

PDF, 636 KB

english, 1999

31

Cutis marmorata telangiectatica congenita: report of 18 cases

M.J.P. Gerritsen, P.M. Steijlen, H.G. Brunner, P. Rieu

Journal:

British Journal of Dermatology

Year:

2000

Language:

english

File:

PDF, 236 KB

english, 2000

32

A case of Rombo syndrome

M.A.M. Van Steensel, N.G.J. Jaspers, P.M. Steijlen

Journal:

British Journal of Dermatology

Year:

2001

Language:

english

File:

PDF, 503 KB

english, 2001

33

Woolly hair, premature loss of teeth, nail dystrophy, acral hyperkeratosis and facial abnormalities: possible new syndrome in a Dutch kindred

M.A.M. Van Steensel, M.I. Koedam, O.Q. Swinkels, F. Rietveld, P.M. Steijlen

Journal:

British Journal of Dermatology

Year:

2001

Language:

english

File:

PDF, 512 KB

english, 2001

34

New syndrome of hypotrichosis, striate palmoplantar keratoderma, acro-osteolysis and periodontitis not due to mutations in cathepsin C

M.A.M. Van Steensel, M. Van Geel, P.M. Steijlen

Journal:

British Journal of Dermatology

Year:

2002

Language:

english

File:

PDF, 324 KB

english, 2002

35

HID and KID syndromes are associated with the same connexin 26 mutation

M. Van Geel, M.A.M. Van Steensel, W. Küster, H.C. Hennies, R. Happle, P.M. Steijlen, A. König‡

Journal:

British Journal of Dermatology

Year:

2002

Language:

english

File:

PDF, 140 KB

english, 2002

36

Connexin 30.3 (GJB4) is not required for normal skin function in humans

M. Van Geel, M.A.M. Van Steensel, P.M. Steijlen

Journal:

British Journal of Dermatology

Year:

2002

Language:

english

File:

PDF, 555 KB

english, 2002

37

Delayed diagnosis of glucagonoma syndrome

Alkemade, Van Tongeren, Van Haelst, Smals, Steijlen, Van De Kerkhof

Journal:

Clinical and Experimental Dermatology

Year:

1999

File:

PDF, 162 KB

1999

38

Spontaneous course of hemangiomas: facts and speculations

Peter Van De Kerkhof, MD, Michette De Rooij, MD, Peter Steijlen, MD

Journal:

International Journal of Dermatology

Year:

1998

Language:

english

File:

PDF, 202 KB

english, 1998

39

Melanocortin 1 Receptor Variants in an Irish Population

Smith, Rachel, Healy, Eugene, Siddiqui, Shazia, Flanagan, Niamh, Steijlen, Peter M, Rosdahl, Inger, Jacques, Jon P, Rogers, Sarah, Turner, Richard, Jackson, Ian J, Birch-Machin, Mark A, Rees, Jonathan

Journal:

The Journal of Investigative Dermatology

Year:

1998

Language:

english

File:

PDF, 236 KB

english, 1998

40

An Atypical Form of Bullous Congenital Ichthyosiform Erythroderma is Caused by a Mutation in the L12 Linker Region of Keratin 1

Kremer, Hannie, Lavrijsen, Adriana P M, McLean, W H Irwin, Lane, E Birgitte, Melchers, Diana, Ruiter, Dirk J, Mariman, Edwin C M, Steijlen, Peter M

Journal:

The Journal of Investigative Dermatology

Year:

1998

Language:

english

File:

PDF, 337 KB

english, 1998

41

A Novel 4 bp Deletion Mutation in the FALDH Gene Segregating in a Turkish Family with Sjögren–Larsson Syndrome

Willemsen, Michel A A P, Steijlen, Peter M, de Jong, Jan G N, Rotteveel, Jan J, IJlst, Lodewijk, van Werkhoven, Michiel A, Wanders, Ronald J A

Journal:

The Journal of Investigative Dermatology

Year:

1999

Language:

english

File:

PDF, 296 KB

english, 1999

42

A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis-Ichthyosis-Deafness Syndrome

van Steensel, Maurice A. M., van Geel, Michel, Nahuys, Marc, Smitt, J. Henk Sillevis, Steijlen, Peter M.

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 247 KB

english, 2002

43

Clouston Syndrome Can Mimic Pachyonychia Congenita

van Steensel, Maurice A.M., Jonkman, Marcel F., van Geel, Michel, Steijlen, Peter M., Irwin McLean, W.H., Smith, Frances J.D.

Journal:

The Journal of Investigative Dermatology

Year:

2003

Language:

english

File:

PDF, 922 KB

english, 2003

44

Topical treatment of ichthyoses and Darier's disease with 13-cis-retinoic acid

P. M. Steijlen, D. O. H. Reifenschweiler, F. C. S. Ramaekers, G. N. P. Muijen, R. Happle, M. Link, D. J. Ruiter, P. C. M. Kerkhof

Journal:

Archives of Dermatological Research

Year:

1993

Language:

english

File:

PDF, 1.80 MB

english, 1993

45

HLA-DR and HLA-DQ antigen expression of anagen and telogen hair bulbs in long-standing alopecia areata

H. Hamm, S. Klemmer, I. Kreuzer, P. M. Steijlen, R. Happle, E. -B. Bröcker

Journal:

Archives of Dermatological Research

Year:

1988

Language:

english

File:

PDF, 804 KB

english, 1988

46

Ichthyosis bullosa of Siemens: Further delineation of the phenotype

P. M. Steijlen, C. M. Perret, J. H. Schuurmans Stekhoven, D. J. Ruiter, R. Happle

Journal:

Archives of Dermatological Research

Year:

1990

Language:

english

File:

PDF, 682 KB

english, 1990

47

CO2laser treatment of benign juvenile acanthosis nigricans

D. S. Wijnberg, H. C. Deutman, P. M. Steijlen, P. H. M. Spauwen

Journal:

European Journal of Plastic Surgery

Year:

2000

Language:

english

File:

PDF, 611 KB

english, 2000

48

Reorganization of the nuclear lamina and cytoskeleton in adipogenesis

Valerie L. R. M. Verstraeten, Johan Renes, Frans C. S. Ramaekers, Miriam Kamps, Helma J. Kuijpers, Fons Verheyen, Martin Wabitsch, Peter M. Steijlen, Maurice A. M. van Steensel, Jos L. V. Broers

Journal:

Histochemistry and Cell Biology

Year:

2011

Language:

english

File:

PDF, 1.70 MB

english, 2011

49

Monoclonal Antibodies Selected to Discriminate Between Malignant Melanomas and Nevocellular Nevi.

Ruiter, Dirk J., Dingjan, Gemma M., Steijlen, Peter M., Van Beveren-Hooyer, Maria, De Graaff-Reitsma, Claire B., Bergman, Wilma, Van Muijen, Goos N. P., Warnaar, Sven O.

Journal:

The Journal of Investigative Dermatology

Year:

1985

File:

PDF, 2.53 MB

1985

50

Immunohistologic Evidence for the Malignant Potential of Congenital Melanocytic Nevi.

Steijlen, Peter M., Hamm, Henning, van Erp, Piet E. J., Johnson, Judith P., Ruiter, Dirk J., Brocker, Eva B.

Journal:

The Journal of Investigative Dermatology

Year:

1989

File:

PDF, 778 KB

1989